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Finasteride may lower depression risk in younger men with hair loss but increase it in older men with prostate issues.

5α-reductase inhibitors may increase the risk of depression and suicidal thoughts.

5-alpha reductase inhibitors slightly increase depression risk, but the risk varies based on the control group used.

5α-reductase inhibitors can cause sexual problems, higher risk of aggressive prostate cancer, and depression.

NDP-MSH protects brain cells and reduces inflammation in Parkinson's disease by activating MC1R and involving Tregs.

Finasteride can cause depression and suicidal thoughts; safer alternatives are recommended.

Montelukast is linked to increased risks of suicidal thoughts and depression.

Androgens increase norepinephrine release, promoting smooth muscle growth in male sex organs, which may contribute to benign prostatic hypertrophy.

Early changes in brain chemicals affect how a drug reduces alcohol intake in rats.

Finasteride may cause depression, suicidal thoughts, and sexual side effects.

Steroid sex hormones activate matriptase in prostate cancer cells but not in breast cancer cells.

Social isolation makes mice more sensitive to alcohol's effects on brain function.

Finasteride reduces response to stress and rewards, affecting behavior and mental health.

Long-term use of a drug for hair loss and prostate issues can cause metabolic problems and depression-like behavior in young male rats.

Neurosteroids affect prolactin levels in sheep differently depending on stress and pregnancy conditions.

Some antidepressants can cause rare hair loss, which can significantly affect patients' well-being.

Plerixafor may help treat pigmentation disorders by promoting skin repigmentation.

Progesterone reduces anxiety without needing progesterone receptors.

Acne patients have higher skin mTORC1 activity, which is reduced by isotretinoin treatment.

Finasteride use may increase suicidality risk, especially in young men.

Low dose finasteride decreases certain steroids, possibly increasing depression risk.

Testosterone treatment may change estrogen receptor methylation in AFAB individuals.

Acne treatment with isotretinoin increases the presence of p53, a protein, in skin and oil glands, which may help reduce acne severity.

Semaglutide may worsen eating disorders in vulnerable individuals.

Antidepressants can cause long-term side effects like severe withdrawal symptoms and sexual dysfunction, which can last for months or years after stopping the medication.

Neuroactive steroids affect cocaine's rewarding effects through the sigma1 receptor.

Peripheral treatments showed some improvement in sexual dysfunction, but central symptoms remain challenging.